784348007: familiaire congenitale spiegelbewegingen (aandoening)

SNOMED CT Concept\Clinical finding (finding)\...

\Finding of movement (finding)\Movement disorder\Mirror movements\Familial congenital mirror movements

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of nervous system\Familial congenital mirror movements
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Familial congenital mirror movements
\Disease\Disorder of foetus and/or newborn\Congenital disease (disorder)\Congenital neurological disorder (disorder)\Familial congenital mirror movements
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Familial congenital mirror movements
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Congenital neurological disorder (disorder)\Familial congenital mirror movements
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Hereditary disorder of nervous system\Familial congenital mirror movements
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Mirror movements\Familial congenital mirror movements
\Disease\Familial disease\Familial congenital mirror movements
\Disease\Movement disorder\Mirror movements\Familial congenital mirror movements

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Familial congenital mirror movements	Occurrence	Congenital	true	Inferred relationship	Some	1
Familial congenital mirror movements	Is a	Hereditary disorder of nervous system	true	Inferred relationship	Some
Familial congenital mirror movements	Finding site	Structure of nervous system (body structure)	true	Inferred relationship	Some	1
Familial congenital mirror movements	Is a	Congenital disease (disorder)	false	Inferred relationship	Some
Familial congenital mirror movements	Is a	Autosomal hereditary disorder	true	Inferred relationship	Some
Familial congenital mirror movements	Is a	Familial disease	true	Inferred relationship	Some
Familial congenital mirror movements	Is a	Mirror movements	true	Inferred relationship	Some
Familial congenital mirror movements	Interprets	Movement	true	Inferred relationship	Some	2
Familial congenital mirror movements	Is a	Congenital neurological disorder (disorder)	true	Inferred relationship	Some

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
3763721016	Familial congenital controlateral synkinesia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3763722011	Hereditary congenital mirror movements	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3763723018	Isolated congenital mirror movements	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3763724012	Familial congenital mirror movements	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3763725013	Hereditary congenital controlateral synkinesia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3763726014	Isolated congenital controlateral synkinesia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3763727017	Familial congenital mirror movements (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
10923261000146110	familiaire congenitale contralaterale synkinesie	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
10965211000146115	familiaire congenitale spiegelbewegingen (aandoening)	nl	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
10965221000146113	familiaire congenitale spiegelbewegingen	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
3763728010	A rare genetic movement disorder with characteristics of involuntary movements on one side of the body that mirror intentional movements on the opposite side of the body, which are present in various first-degree members of a family, persist beyond the first decade of life, and have no associated comorbidities.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core